The role of gene copy number variation in antimicrobial resistance in human fungal pathogens.

npj antimicrobials and resistance Pub Date : 2025-01-06 eCollection Date: 2025-01-01 DOI:10.1038/s44259-024-00072-1
Adarsh Jay, David F Jordan, Aleeza Gerstein, Christian R Landry
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Abstract

Faced with the burden of increasing resistance to antifungals in many fungal pathogens and the constant emergence of new drug-resistant strains, it is essential to assess the importance of various resistance mechanisms. Fungi have relatively plastic genomes and can tolerate genomic copy number variation (CNV) caused by aneuploidy and gene amplification or deletion. In many cases, these genomic changes lead to adaptation to stressful conditions, including those caused by antifungal drugs. Here, we specifically examine the contribution of CNVs to antifungal resistance. We undertook a thorough literature search, collecting reports of antifungal resistance caused by a CNV, and classifying the examples of CNV-conferred resistance into four main mechanisms. We find that in human fungal pathogens, there is little evidence that gene copy number plays a major role in the emergence of antifungal resistance compared to other types of mutations. We discuss why we might be underestimating their importance and new approaches being used to study them.

基因拷贝数变异在人类真菌病原菌抗微生物药物耐药性中的作用。
面对许多真菌病原体对抗真菌药物的耐药性不断增加和新的耐药菌株不断出现的负担,有必要评估各种耐药机制的重要性。真菌具有相对可塑性的基因组,能够耐受非整倍体和基因扩增或缺失引起的基因组拷贝数变异。在许多情况下,这些基因组变化导致对压力条件的适应,包括抗真菌药物引起的压力条件。在这里,我们专门研究了CNVs对抗真菌抗性的贡献。我们进行了全面的文献检索,收集了由CNV引起的抗真菌耐药性的报告,并将CNV产生耐药性的例子分为四种主要机制。我们发现,在人类真菌病原体中,与其他类型的突变相比,很少有证据表明基因拷贝数在抗真菌耐药性的出现中起主要作用。我们讨论了为什么我们可能低估了它们的重要性,以及用于研究它们的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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